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				<datestamp>2011-09-30T03:44:50Z</datestamp>
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	<dc:title xml:lang="en-US">Synthesis and optimization of methyl 5-acetyl-1,4-dihydro-2,6-dimethyl-4-(substituent benzylidene)pyridine-3-carboxylate</dc:title>
	<dc:creator>Liu, Rui Dong</dc:creator>
	<dc:creator>Zhang, Jian</dc:creator>
	<dc:subject xml:lang="en-US">Unsymmetrical</dc:subject>
	<dc:subject xml:lang="en-US">1</dc:subject>
	<dc:subject xml:lang="en-US">4-dihydro-Hantzsch pyridine</dc:subject>
	<dc:subject xml:lang="en-US">Condensation</dc:subject>
	<dc:subject xml:lang="en-US">Catalyst</dc:subject>
	<dc:subject xml:lang="en-US">Cyclization</dc:subject>
	<dc:subject xml:lang="en-US">Polar aprotic solvent</dc:subject>
	<dc:description xml:lang="en-US">Two 1,4-dihydro-Hantzsch pyridine derivatives were synthesized by three steps. In the condensation step, the reaction time can be shortened to 1.5 h through using H2SO4-acetic anhydride system as a catalyst rather than the acetic acid-piperidine systemin the cyclization step, the reaction time was shortened from 20 h in ethanol to 15 h in polar aprotic solvent, and the yield of two products also was increased from 43.3% and 39.7% in traditional solvent to 93.2% and 90.1% in polar aprotic solvent.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-09-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/126</dc:identifier>
	<dc:identifier>10.5155/eurjchem.2.3.308-310.126</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 3 (2011): September 2011; 308-310</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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